US2007122338A1PendingUtilityA1

Positive active material for lithium secondary battery and a method of preparing the same

Assignee: PARK HONG-KYUPriority: Mar 13, 2001Filed: Dec 22, 2006Published: May 31, 2007
Est. expiryMar 13, 2021(expired)· nominal 20-yr term from priority
H01M 4/131H01M 4/1391H01M 4/505H01M 4/366H01M 4/525Y02P70/50H01M 10/0525H01M 4/48H01M 4/04Y02E60/10
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Claims

Abstract

Disclosed is a positive active material for a lithium secondary battery and a preparation method of the same, in particular a positive active material and preparation method of the same that can improve cycle-life characteristics at a high temperature and room temperature, and storage characteristics at a high temperature. The present invention has the effect of providing a positive active material and preparation method of the same that can improve cycle-life characteristics at room temperature and at a high temperature, and storage characteristics at a high temperature, by coating the surface of the lithium manganese spinel oxide particles with a lithium metal complex oxide.

Claims

exact text as granted — not AI-modified
1 . A preparation method of a positive active material for a lithium secondary battery comprising; 
 a) supplying lithium manganese spinel oxide of the following Formula 1;    b) coating the lithium manganese spinel oxide of a) with an overlayer material compound of the following Formula 2, comprising: 
 i) a lithium compound;  
 ii) a nickel compound; and  
 iii) a metal compound comprising metal Me selected from the group consisting of Ni, Mn, Co, V, Ti, Zr, Cr, Al, Mg, Fe, Cu, Zn, Ga, and Gd; and  
   c) sintering the lithium manganese spinel oxide of a) coated with the overlayer material of b);      Li 1+x Mn 2-x-y M y O 4+d    Formula 1    wherein,    M is selected from the group consisting of Ti, V, Cr, Co, Ni, Mg, Zr, Fe, Gd, and Ga;    x is a real number of 0-0.12;    y is a real number of 0-0.5; and    d is a real number of 0-0.04;      LiNi 1-z Me z O 2    Formula 2    wherein,    Me is selected from the group consisting of of Ni, Mn, Co, V, Ti, Zr, Cr, Al, Mg, Fe, Cu, Zn, Ga, and Gd; and    z is a real number of 0-0.7.    
   
   
       2 . The preparation method of  claim 1  wherein the lithium manganese spinel oxide of a) is made by heating a mixture of a lithium compound selected from the group consisting of 
 LiOH, LiOH.H 2 O, LiCH 3 COO, LiCHO 2 , LiCHO 2 .H 2 O, Li 2 SO 4 . and LiNO 3 ; and a    manganese compound selected from the group consisting of MnO 2 , MnCO 2 , Mn(CH 3 COO) 2 , MnSO 4 , Mn(NO 3 ) 2 , and Mn(OH) 2  under the condition of air or a complex gas comprising over 2 wt % of oxygen for 1 to 50 hours at 400 to 900° C.    
   
   
       3 . The preparation method of  claim 2  wherein the lithium manganese spinel oxide further comprises a metal compound comprising metal M selected from the group consisting Ni, Mn, Co, V, Ti, Zr, Cr, Al, Mg, Fe, Cu, Zn, Ga, and Gd.  
   
   
       4 . The preparation method of  claim 3  wherein the metal compound comprising metal M is selected from the group consisting of carbonate salt, nitrate salt, hydrate salt, sulfate salt, acetate salt, citric acid salt and chloride of metal M.  
   
   
       5 . The preparation method of  claim 1  wherein the lithium compound of b) is selected from the group consisting of LiOH, LiOH.H 2 O, LiCH 3 COO, LiCHO 2 , LiCHO 2 .H 2 O, Li 2 SO 4 and LiNO 3.    
   
   
       6 . The preparation method of  claim 1  wherein the nickel compound of b) is selected from the group consisting of carbonate salt, nitrate salt, hydrate salt, sulfate salt, acetate salt, citric acid salt and chloride of nickel.  
   
   
       7 . The preparation method of  claim 1  wherein the metal compound comprising metal Me of b) is selected from the group consisting of carbonate salt, nitrate salt, hydrate salt, sulfate salt, acetate salt, citric acid salt and chloride of Me.  
   
   
       8 . The preparation method of  claim 1  wherein the overlayer material of compound by the following Formula 2 is coated on the lithium manganese spinel oxide to make a quantity of the overlayer produced after the sintering of c) to be 0.05 to 50 mol % of the lithium manganese spinel oxide,  
       LiNi 1-z Me z O 2    Formula 2  wherein,    Me is selected from the group consisting of Ni, Co, V, Ti, Zr, Cr, Al, Cu, Zn, Ga, and Gd; and    z is a real number of 0-0.7.    
   
   
       9 . The preparation method of  claim 1  wherein the sintering of c) is done by heat-treating the coated lithium manganese complex oxide under 0.05 to 3.0 l/gH of air or complex gas of over 10 wt % of oxygen for 1 to 30 hours at 400 to 900° C.  
   
   
       10 . The lithium secondary battery comprising the positive active material made by the preparation method of  claim 1.

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